WO2017080318A1 - Composition pour électronique imprimée, dispositif électronique la comprenant, et procédé de préparation d'un film mince de matériau fonctionnel - Google Patents

Composition pour électronique imprimée, dispositif électronique la comprenant, et procédé de préparation d'un film mince de matériau fonctionnel Download PDF

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WO2017080318A1
WO2017080318A1 PCT/CN2016/099785 CN2016099785W WO2017080318A1 WO 2017080318 A1 WO2017080318 A1 WO 2017080318A1 CN 2016099785 W CN2016099785 W CN 2016099785W WO 2017080318 A1 WO2017080318 A1 WO 2017080318A1
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group
solvent
printed electronic
functional material
printing
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PCT/CN2016/099785
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English (en)
Chinese (zh)
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潘君友
杨曦
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广州华睿光电材料有限公司
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Priority to CN201680059913.8A priority Critical patent/CN108137972B/zh
Publication of WO2017080318A1 publication Critical patent/WO2017080318A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/02—Printing inks
    • C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
    • C09D11/033—Printing inks characterised by features other than the chemical nature of the binder characterised by the solvent

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  • the present invention relates to a printed electronic composition comprising a composition comprising at least one functional material and at least one olefin, particularly a terpene solvent.
  • the invention further relates to a method of making an electronic device and a functional material film comprising the printed electronic composition.
  • the organic light-emitting diode which is a new-generation display technology
  • OLED organic light-emitting diode
  • FMM fine mask
  • Low yield In order to solve the above problems, techniques for realizing high-resolution full-color display using a printing process have received increasing attention. For example, inkjet printing can produce functional material films in a large area and at low cost. Compared with traditional semiconductor production processes, inkjet printing has low energy consumption, low water consumption, and environmental protection, and is a production technology with great advantages and potential.
  • QLED quantum dot light-emitting diode
  • Organic semiconductor materials have gained widespread attention and significant progress in their use in electronic and optoelectronic devices due to their solution processability.
  • Solution processability allows the organic functional material to form a thin film of the functional material in the device by certain coating and printing techniques. Such a technology can effectively reduce the processing cost of electronic and optoelectronic devices, and meet the process requirements of large-area preparation.
  • KATEEVA discloses an ester solvent-based organic small molecule material ink for printing OLEDs (US2015044802A1)
  • UNIVERSAL DISPLAY CORPORATION discloses A printable organic small molecular material ink based on an aromatic ketone or aromatic ether solvent (US20120205637)
  • SEIKO EPSON CORPORATION discloses a printable organic polymer material ink based on a substituted benzene derivative solvent.
  • printing inks involving organic functional materials are: CN102408776A, CN103173060A, CN103824959A, CN1180049C, CN102124588B, US2009130296A1, US2014097406A1, and the like.
  • Quantum dots are nano-sized semiconductor materials with quantum confinement effects. When stimulated by light or electricity, quantum dots emit fluorescence with specific energy. The color (energy) of fluorescence is determined by the chemical composition and size of quantum dots. Therefore, the control of the size and shape of quantum dots can effectively regulate its electrical and optical properties.
  • countries are studying the application of quantum dots in full color, mainly in the display field.
  • quantum dots as electroluminescent devices (QLEDs) have been rapidly developed, and device lifetimes have been greatly improved, as in Peng et al., Nature Vol515 96 (2015) and Qian et al., in Nature Photonics Vol 9 259 ( Reported in 2015).
  • Nanoco Technologies Ltd. discloses a method for printing a printable ink formulation comprising nanoparticles (CN101878535B).
  • Printable nanoparticle inks and corresponding nanoparticle-containing films are obtained by selecting suitable solvents such as toluene and dodecyl selenol; Samsung Electronics discloses a quantum dot ink for inkjet printing. (US8765014B2).
  • the ink contains a concentration of quantum dot material, an organic solvent, and an alcohol polymer additive having a high viscosity.
  • a quantum dot film is obtained by printing the ink, and a quantum dot electroluminescent device is prepared;
  • QD Vision, Inc. discloses a quantum dot ink formulation comprising a host material, a quantum dot Materials and an additive (US2010264371A1).
  • R 1 and R 2 are each independently selected from H, D, a linear alkyl group having 1 to 20 C atoms, an alkoxy group or a thioalkoxy group, and having 3 to 20 C atoms. a chain or cyclic alkyl, alkoxy or thioalkoxy group, a silyl group, a substituted keto group having 1 to 20 C atoms, an alkane having 2 to 20 C atoms An oxycarbonyl group, an aryloxycarbonyl group having 7 to 20 C atoms, a cyano group, a carbamoyl group, a haloformyl group, a formyl group, an isocyano group, an isocyanate a group, a thiocyanate group or an isothiocyanate group, a hydroxyl group, a nitro group, a CF 3 group, Cl, Br, F, a substituted or unsubstituted having 5 to 40 ring atoms An
  • the olefinic solvent has a viscosity at 25 ° C in the range of 1 cPs to 100 cPs. According to some preferred embodiments of the invention, the olefinic solvent has a surface tension at 25 ° C in the range of 19 dyne / cm to 50 dyne / cm.
  • the olefinic solvent is a terpene, that is, a terpene compound or a terpene compound substituted with one or more alcohol group, ester group, ether group, ketone group or aldehyde group. .
  • the olefinic solvent is selected from the group consisting of monoterpenes.
  • the olefinic solvent is selected from the group consisting of terpinolene, terpene or alpha-terpineol or mixtures thereof.
  • At least one other solvent is further included, and the olefin solvent accounts for more than 50% by weight based on the total weight of the mixed solvent.
  • the at least one other solvent is selected from the group consisting of aromatic or heteroaromatic based solvents, alcohol based, ether based, keto based, ester based or aldehyde based solvents.
  • the functional material is an inorganic nanomaterial.
  • the functional material is a quantum dot material, i.e., its particle size has a monodisperse size distribution selected from a different nanotopography of a sphere, cube, rod or branched structure.
  • the functional material is a luminescent quantum dot material having an emission wavelength between 380 nm and 2500 nm.
  • another inorganic functional material is further included, selected from Group IV, Group II-VI, Group II-V, Group III-V, Group III-VI, IV-VI of the Periodic Table of the Elements.
  • the functional material is a perovskite nanoparticle material.
  • the functional material is a luminescent perovskite nanomaterial, a metal nanoparticle material, a metal oxide nanoparticle material, or a mixture thereof.
  • the functional material is an organic functional material.
  • the organic functional material is selected from the group consisting of a hole injecting material, a hole transporting material, an electron transporting material, an electron injecting material, an electron blocking material, a hole blocking material, an illuminant, a host material or Organic dyes.
  • the organic functional material comprises at least one host material and at least one illuminant.
  • the functional material is from 0.3% to 30% by weight, and the olefinic solvent is from 70% to 99.7% by weight.
  • Another object of the present invention is to provide an electronic device comprising a functional layer printed or coated from a printed electronic composition as described above, wherein the olefinic solvent is capable of being combined from the printed electronic The material evaporates to form a thin film of functional material.
  • the electronic device is selected from the group consisting of a quantum dot light emitting diode, a quantum dot photovoltaic cell, a quantum dot luminescent cell, a quantum dot field effect transistor, a quantum dot luminescence field effect transistor, a quantum dot laser, a quantum dot Sensors, organic light-emitting diodes, organic photovoltaic cells, organic light-emitting cells, organic field effect transistors, organic light-emitting FETs, organic lasers or organic sensors.
  • Another object of the present invention is to provide a method for preparing a functional material film, wherein the printed electronic composition as described above is applied to a substrate by printing or coating, wherein the printing or coating method Selected from inkjet printing, jet printing, typography, screen printing, dip coating, spin coating, knife coating, roller printing, torsion roll printing, lithography, flexographic printing, rotary printing, spray coating, brushing or Pad printing, or slit type extrusion coating.
  • the present invention provides a printed electronic composition which can adjust the viscosity and surface tension to a suitable range in accordance with a specific printing method, particularly ink jet printing, to facilitate printing, and to form a film having a uniform surface.
  • the solvent can be effectively removed by post-treatment, such as heat treatment or vacuum treatment, which is beneficial to ensure the performance of the electronic device.
  • the present invention therefore provides a printing ink for the preparation of high quality functional films, in particular printing inks comprising quantum dots and organic semiconductor materials, providing a technical solution for printed electronic or optoelectronic devices.
  • FIG. 1 is a structural view of a preferred light-emitting device according to the present invention, in which 101 is a substrate, 102 is an anode, 103 is a hole injection layer (HIL) or a hole transport layer (HTL), and 104 is a light-emitting layer (electrical A light-emitting device) or a light absorbing layer (photovoltaic cell), 105 is an electron injection layer (EIL) or an electron transport layer (ETL), and 106 is a cathode.
  • HIL hole injection layer
  • HTL hole transport layer
  • 104 is a light-emitting layer (electrical A light-emitting device) or a light absorbing layer (photovoltaic cell)
  • 105 is an electron injection layer (EIL) or an electron transport layer (ETL)
  • 106 is a cathode.
  • the present invention provides a printed electronic composition comprising a composition comprising at least one functional material and at least one olefinic solvent.
  • the olefinic solvent has a viscosity at 25 ° C, a range of from 1 cPs to 100 cPs, a surface tension at 25 ° C, a range of from 19 dyne/cm to 50 dyne/cm, and a boiling point of greater than 150 ° C.
  • the invention further relates to a method of making an electronic device and a functional material film comprising the printed electronic composition.
  • the present invention provides a printed electronic composition comprising at least one functional material and at least one olefinic solvent, said olefinic solvent having the structure of formula (I):
  • the organic solvent has a boiling point of ⁇ 120 ° C and can be evaporated from a solvent system to form a film of a functional material.
  • the printed electronic composition according to the invention comprises an olefinic solvent of the formula (I), wherein R 1 , R 2 are H, or D, or from 1 to 10, more preferably a linear alkyl, alkoxy or thioalkoxy group of 1 to 5 C atoms, or a branched or cyclic alkyl group having 3 to 10, more preferably 3 to 5 C atoms,
  • the printed electronic composition according to the invention comprises an olefinic solvent of the formula (I) wherein at least one of R 1 , R 2 is selected from an aromatic or heteroaromatic group.
  • Suitable aromatic or heteroaromatic groups may preferably be selected from the following structural units:
  • the molecular weight needs to be in an appropriate range.
  • the printed electronic composition according to the present invention, wherein the olefinic solvent according to formula (I) has a molecular weight of from 100 to 350 Dalton, preferably from 120 to 330 Dalton, more preferably from 140 to 310 Dalton. More preferably, it is at 160-280 Dalton, preferably at 180-250 Dalton.
  • the olefinic solvent contained in the printed electronic composition according to the present invention is terpene.
  • a terpene refers to a terpene compound or a terpene compound substituted with one or more groups such as an alcohol group, an ester group, an ether group, a ketone group or an aldehyde group.
  • the terpene compound is a generic term for a series of terpenoids, and is an olefin compound having an integral multiple of isoprene, and is a chain or cyclic olefin of the formula (C 5 H 8 )n. class.
  • Terpenoids are hydrocarbons that can be divided into several isoprene structural units.
  • the molecular formula has a simple multiple relationship with isoprene.
  • the general formula can be written as (C 5 H 8 )n.
  • terpenoids it can be divided into monoterpenes (consisting of two isoprene units), sesquiterpenes (consisting of three isoprene units), and diterpene (consisting of four isoprene units). ), sesquiterpene (consisting of five isoprene units), triterpenoid (composed of six isoprene units), tetraterpene (consisting of eight isoprene units), polypyrene ( It consists of more than eight isoprene units).
  • the olefin-based organic solvent used to dissolve the functional material is selected to take into account its boiling point parameters.
  • the olefinic organic solvent contained in the printed electronic composition according to the present invention has a boiling point of at least 150 °C.
  • the olefin-based organic solvent has a boiling point ⁇ 180 ° C; in certain embodiments, the olefin-based organic solvent has a boiling point ⁇ 200 ° C; in certain embodiments
  • the olefin-based organic solvent has a boiling point of ⁇ 250 ° C; in other preferred embodiments, the olefin-based organic solvent has a boiling point of ⁇ 275 ° C or ⁇ 300 ° C.
  • the boiling points within these ranges are beneficial for preventing nozzle clogging of the inkjet printhead.
  • the olefin-based organic solvent can be evaporated from a solvent system to form a film comprising a functional material.
  • a printed electronic composition according to the present invention comprises an olefin-based organic solvent having a surface tension at 25 ° C in the range of 19 dyne / cm to 50 dyne / cm.
  • the olefin-based organic solvent used to dissolve the functional material should be considered for its surface tension parameter. Suitable ink surface tension parameters are suitable for a particular substrate and a particular printing method.
  • the olefin-based organic solvent has a surface tension at 25 ° C ranging from about 19 dyne/cm to 50 dyne/cm; in a more preferred embodiment
  • the surface temperature of the olefin-based organic solvent at 25 ° C is in the range of about 22 dyne / cm to 35 dyne / cm; in a most preferred embodiment, the olefin-based organic solvent is at 25 ° C
  • the surface tension is in the range of about 25 dyne/cm to 33 dyne/cm.
  • the ink according to the invention has a surface tension at 25 ° C in the range of from about 19 dyne/cm to 50 dyne/cm; more preferably in the range of from 22 dyne/cm to 35 dyne/cm; preferably in 25 dyne/ Cm to the 33dyne/cm range.
  • a printed electronic composition according to the present invention comprises an olefin-based organic solvent having a viscosity at 25 ° C in the range of 1 cPs to 100 cPs.
  • the olefin-based organic solvent has a viscosity of less than 100 cps; in a more preferred embodiment, the olefin-based organic solvent has a viscosity of less than 50 cps; In a most preferred embodiment, the olefin-based organic solvent has a viscosity of from 1.5 to 20 cps.
  • the viscosity can also be adjusted by the concentration of the functional material in the ink.
  • the solvent system comprising an olefin-based organic solvent according to the present invention facilitates the adjustment of the printing ink to an appropriate range in accordance with the printing method used.
  • the printed electronic composition according to the present invention comprises a functional material in a weight ratio ranging from 0.3% to 30% by weight, preferably from 0.5% to 20% by weight, more preferably from 0.5% to 15% by weight, most preferably It is in the range of 0.5% to 10% by weight.
  • the printed electronic composition according to the present invention has a viscosity at 25 ° C of about 1 cps to 100 cps when it is formulated according to the above ratio; more preferably in the range of 1 cps to 50 cps; It is in the range of 1.5cps to 20cps.
  • the viscosity herein refers to the viscosity at ambient temperature at the time of printing, and is usually 15 to 30 ° C, preferably 18 to 28 ° C, more preferably 20 to 25 ° C, and most preferably 23 to 25 ° C.
  • the printed electronic composition so formulated will be particularly suitable for ink jet printing.
  • the ink obtained by the olefin-based solvent system satisfying the above boiling point and surface tension parameters and viscosity parameters can form a functional material film having uniform thickness and composition properties.
  • a printed electronic composition according to the present invention comprises an olefinic solvent which is monoterpene.
  • a printed electronic composition according to the present invention comprises an olefin solvent selected from, but not limited to, the following: terpinolene, terpene or alpha-terpineol .
  • the olefinic solvent system comprises a single terpene compound.
  • a printed electronic composition according to the present invention comprises a mixture of two or more olefinic compounds.
  • a printed electronic composition according to the present invention further comprises at least one other solvent, and the olefinic solvent comprises more than 50% by weight based on the total weight of the mixed solvent.
  • the organic solvent comprising olefins comprises at least 70% by weight of the total solvent; more preferably, the organic solvent comprising olefins comprises at least 80% by weight of the total solvent.
  • the olefin-based solvent system comprises at least 90% by weight of an olefinic organic solvent, or consists essentially of an organic solvent of an olefin, or consists entirely of an organic solvent of an olefin.
  • a printed electronic composition according to the present invention comprising at least one other solvent as described above is selected from the group consisting of aromatic or heteroaromatic solvents represented by the following formula (II) :
  • Ar 1 is an aromatic or heteroaryl ring having 5 to 10 carbon atoms, n ⁇ 0, and R is a substituent.
  • An aromatic group refers to a hydrocarbon group containing at least one aromatic ring, including a monocyclic group and a polycyclic ring system.
  • a heteroaromatic group refers to a hydrocarbon group (containing a hetero atom) comprising at least one heteroaromatic ring, including a monocyclic group and a polycyclic ring system.
  • These polycyclic rings may have two or more rings in which two carbon atoms are shared by two adjacent rings, a fused ring. At least one of these rings of the polycyclic ring is aromatic or heteroaromatic.
  • examples of the aromatic group are: benzene, naphthalene, anthracene, phenanthrene, perylene, tetracene, anthracene, benzofluorene, triphenylene, anthracene, anthracene, and derivatives thereof.
  • heteroaromatic groups are: furan, benzofuran, thiophene, benzothiophene, pyrrole, pyrazole, triazole, imidazole, oxazole, oxadiazole, thiazole, tetrazole, anthracene, anthracene Oxazole, pyrroloimidazole, pyrrolopyrrole, thienopyrrole, thienothiophene, furopyrrol, furanfuran, thienofuran, benzisoxazole, benzopyrene Thiazole, benzimidazole, pyridine, pyrazine, pyridazine, pyrimidine, triazine, quinoline, isoquinoline, o-diazepine, quinoxaline, phenanthridine, pyridine, quinazoline, quinazolinone, And its derivatives.
  • the total number of atoms other than H in all the substituents R in the above formula (II) is greater than or equal to 1, preferably from 2 to 20, more preferably from 2 to 10, most preferably from 3 to 10.
  • the atoms other than H in all the substituents R described herein include atoms of C, Si, N, P, O, S, F, Cl, Br, I and the like.
  • a methoxy substituent and three chlorine substituents are all included in the scope of the benzene invention, and specific examples are 1-methoxynaphthalene and trichlorobenzene.
  • the substituted aromatic or heteroaromatic solvent has a boiling point of ⁇ 100 ° C, preferably ⁇ 140 ° C, more preferably ⁇ 180 ° C, most preferably ⁇ 200 ° C.
  • organic solvent of formula (I) as described above may be further selected from the following formula:
  • X is CR 4 or N
  • Ar 1 in formula (II) is preferably selected from the group consisting of:
  • one or more of the groups R in the above formula (II) may form a monocyclic or polycyclic aliphatic or aromatic group with each other and/or a ring bonded to the group. Ring system.
  • solvents are, but are not limited to, 1- Tetrahydronaphthalenone, 2-tetralone, 1-methoxynaphthalene, 2-methoxynaphthalene, tetrahydronaphthalene, 1-chloronaphthalene, 2-chloronaphthalene, 1,4-dimethylnaphthalene, 1 - Methylnaphthalene, 2-methylnaphthalene, and the like.
  • aromatic or heteroaromatic solvents suitable for use with the printing inks of the present invention are, but are not limited to, p-cymene, 3,4,5-trimethyltoluene, 1-tetralone , 3-phenoxytoluene, acetophenone, 1-methoxynaphthalene, p-diisopropylbenzene, pentylbenzene, tetrahydronaphthalene, cyclohexylbenzene, chloronaphthalene, 1,4-dimethylnaphthalene, 3 -isopropylbiphenyl, p-methylisopropylbenzene, dipentylbenzene, o-diethylbenzene, m-diethylbenzene, p-diethylbenzene, 1,2,3,4-tetramethylbenzene, 1,2,3, 5-tetramethylbenzene, 1,2,4,5-tetramethylbenzene, butylbenzen
  • a printed electronic composition according to the present invention further comprises an aromatic or heteroaromatic solvent such as p-cymene, 3,4,5-trimethyl. Toluene, 1-tetralone or 3-phenoxytoluene.
  • a printed electronic composition according to the present invention further comprises at least one other solvent, wherein said one other solvent may be selected from the group consisting of an alcohol group or an ether group or a ketone group or ester. Base or aldehyde based solvent.
  • a printed electronic composition according to the present invention further comprises another organic solvent.
  • organic solvents include, but are not limited to, methanol, ethanol, 2-methoxyethanol, dichloromethane, chloroform, chlorobenzene, o-dichlorobenzene, tetrahydrofuran, anisole, morpholine, toluene, O-xylene, m-xylene, p-xylene, 1,4 dioxane, acetone, methyl ethyl ketone, 1,2 dichloroethane, 3-phenoxytoluene, 1,1,1 -trichloroethane, 1,1,2,2-tetrachloroethane, ethyl acetate, butyl acetate, dimethylformamide, dimethylacetamide, dimethyl sulfoxide, tetrahydronaphthalene, naphthalene Alkanes, hydrazines and/or mixtures thereof.
  • the olefin-based solvent system can effectively dissolve a functional material, that is, a solvent for replacing a conventionally used dissolution functional material as a new solvent, such as toluene, xylene, chloroform, chlorobenzene, dichlorobenzene, n-heptane. Wait.
  • a functional material that is, a solvent for replacing a conventionally used dissolution functional material as a new solvent, such as toluene, xylene, chloroform, chlorobenzene, dichlorobenzene, n-heptane. Wait.
  • the printing ink may further comprise one or more components such as surface active compounds, lubricants, wetting agents, dispersing agents, hydrophobic agents, adhesives, etc., for adjusting viscosity, film forming properties, and improving adhesion. Wait.
  • the printing ink can be deposited into a functional film by a variety of printing or coating techniques, including, but not limited to, ink jet printing, Nozzle Printing, typography, screen printing, Dip coating, spin coating, blade coating, roll printing, torsion roll printing, lithography, flexographic printing, rotary printing, spraying, brushing or pad printing, slit type extrusion coating, and the like.
  • Preferred printing techniques are ink jet printing, jet printing and gravure printing.
  • Helmut Kipphan's "Printing Media Handbook: Techniques and Production Methods” Handbook of Print Media: Technologies and Production Methods).
  • printing inks suitable for inkjet printing require adjustment of the surface tension, viscosity, and wettability of the ink so that the ink can be ejected through the nozzle at a printing temperature (such as room temperature, 25 ° C) without being sprayed. Drying on the nozzle or clogging the nozzle, or forming a continuous, flat and defect-free film on a particular substrate.
  • the printed electronic composition according to the invention comprises at least one functional material.
  • the functional material preferably refers to a material having certain photoelectric functions.
  • Photoelectric functions include, but are not limited to, hole injection function, hole transport function, electron transport function, electron injection function, electron blocking function, hole blocking function, light emitting function, main body function and light absorbing function.
  • the corresponding functional materials are called hole injection material (HIM), hole transport material (HTM), electron transport material (ETM), electron injecting material (EIM), electron blocking material (EBM), hole blocking material (HBM). ), Emitter, Host and Organic Dyes.
  • the functional material may be an organic material or an inorganic material.
  • the printed electronic composition according to the invention comprises at least one functional material that is an inorganic nanomaterial.
  • the at least one inorganic nano material is an inorganic semiconductor nanoparticle material.
  • the inorganic nanomaterial has an average particle diameter in the range of about 1 to 1000 nm. In certain preferred embodiments, the inorganic nanomaterials have an average particle size of from about 1 to 100 nm. In certain more preferred embodiments, the inorganic nanomaterial has an average particle size of from about 1 to 20 nm, preferably from 1 to 10 nm.
  • the inorganic nanomaterials may be selected from different shapes including, but not limited to, different nanotopography such as spheres, cubes, rods, discs or branched structures, as well as mixtures of particles of various shapes.
  • the inorganic nanomaterial is a quantum dot material having a very narrow, monodisperse size distribution, i.e., the size difference between the particles and the particles is very small.
  • the deviation of the monodisperse quantum dots in the size of the root mean square is less than 15% rms; more preferably, the deviation of the monodisperse quantum dots in the size of the root mean square is less than 10% rms; optimally, monodisperse Quantum dots have a root mean square deviation of less than 5% rms in size.
  • the inorganic nanomaterial is a luminescent material.
  • the luminescent inorganic nanomaterial is a quantum dot luminescent material.
  • luminescent quantum dots can illuminate at wavelengths between 380 nanometers and 2500 nanometers.
  • the luminescent wavelength of a quantum dot having a CdS core is in the range of about 400 nm to 560 nm; the luminescent wavelength of a quantum dot having a CdSe nucleus is in the range of about 490 nm to 620 nm; the luminescent wavelength of a quantum dot having a CdTe core Located in the range of about 620 nm to 680 nm; the quantum wavelength of the quantum dots having the InGaP core is in the range of about 600 nm to 700 nm; the wavelength of the quantum dots having the PbS core is in the range of about 800 nm to 2500 nm; the quantum having the PbSe nucleus
  • the illuminating wavelength of the point is in the range of about 1200 nm to 2500 nm; the luminescent wavelength of the quantum dot having the
  • the quantum dot material comprises at least one blue light having a peak wavelength of 450 nm to 460 nm, or green light having a peak wavelength of 520 nm to 540 nm, or a peak wavelength of 615 nm to 630 nm. Red light, or a mixture of them.
  • the quantum dots contained may be selected from a particular chemical composition, topographical structure, and/or size to achieve light that emits the desired wavelength under electrical stimulation.
  • a relationship between the luminescent properties of quantum dots and their chemical composition, morphology, and/or size see Annual Review of Material Sci., 2000, 30, 545-610; Optical Materials Express., 2012, 2, 594-628; Nano Res, 2009, 2, 425-447. The entire contents of the above-listed patent documents are hereby incorporated by reference.
  • the narrow particle size distribution of the quantum dots enables quantum dots to have a narrower luminescence spectrum (J. Am. Chem. Soc., 1993, 115, 8706; US 20150108405). Furthermore, depending on the chemical composition and structure employed, the size of the quantum dots needs to be adjusted accordingly within the above-described size range to achieve the luminescent properties of the desired wavelength.
  • the luminescent quantum dots are semiconductor nanocrystals.
  • semiconductor nanocrystals range in size from about 2 nanometers to about 15 nanometers.
  • the size of the quantum dots needs to be adjusted accordingly within the above-described size range to achieve the luminescent properties of the desired wavelength.
  • the semiconductor nanocrystal includes at least one semiconductor material, wherein the semiconductor material may be selected from Group IV, II-VI, II-V, III-V, III-VI, IV-VI of the periodic table, Group I-III-VI, Group II-IV-VI, Group II-IV-V binary or multi-component semiconductor compounds or mixtures thereof.
  • the semiconductor material include, but are not limited to, Group IV semiconductor compounds composed of elemental Si, Ge, and binary compounds SiC, SiGe; Group II-VI semiconductor compounds, including binary compounds including CdSe, CdTe, CdO, CdS, CdSe, ZnS, ZnSe, ZnTe, ZnO, HgO, HgS, HgSe, HgTe, ternary compounds including CdSeS, CdSeTe, CdSTe, CdZnS, CdZnSe, CdZnTe, CgHgS, CdHgSe, ZnSeS, ZnSeTe, ZnSTe, HgSeS, HgSeTe, HgSTe, HgZnS, HgSeSe, and quaternary compounds include CgHgSeS, CdHgSeTe, CgHgSTe, CdZnSeS, CdZnS, C
  • the luminescent quantum dots comprise a Group II-VI semiconductor material, preferably selected from the group consisting of CdSe, CdS, CdTe, ZnO, ZnSe, ZnS, ZnTe, HgS, HgSe, HgTe, CdZnSe, and any combination thereof.
  • this material is used as a luminescent quantum dot for visible light due to the relatively mature synthesis of CdSe due to CdSe.
  • the luminescent quantum dots comprise a Group III-V semiconductor material, preferably selected from the group consisting of InAs, InP, InN, GaN, InSb, InAsP, InGaAs, GaAs, GaP, GaSb, AlP, AlN, AlAs, AlSb , CdSeTe, ZnCdSe and any combination thereof.
  • a light emitting quantum dot including Group IV-VI semiconductor material preferably selected from PbSe, PbTe, PbS, PbSnTe, Tl 2 SnTe 5 , and any combination thereof.
  • the quantum dots are a core-shell structure.
  • the core and the shell respectively comprise one or more semiconductor materials, either identically or differently.
  • the core of the quantum dot may be selected from the group IV, II-VI, II-V, III-V, III-VI, IV-VI, I-III-VI of the periodic table, Group II-IV-VI, Group II-IV-V binary or multi-element semiconductor compounds.
  • quantum dot nuclei include, but are not limited to, ZnO, ZnS, ZnSe, ZnTe, CdO, CdS, CdSe, CdTe, MgS, MgSe, GaAs, GaN, GaP, GaSe, GaSb, HgO, HgS, HgSe, An alloy or mixture of HgTe, InAs, InN, InSb, AlAs, AlN, AlP, AlSb, PbO, PbS, PbSe, PbTe, Ge, Si, and any combination thereof.
  • the shell of the quantum dot comprises a semiconductor material that is the same or different from the core.
  • Semiconductor materials that can be used for the shell include Group IV, II-VI, II-V, III-V, III-VI, IV-VI, I-III-VI, II-IV-VI of the Periodic Table of the Elements. Group, II-IV-V binary or multi-component semiconductor compounds.
  • quantum dot nuclei include, but are not limited to, ZnO, ZnS, ZnSe, ZnTe, CdO, CdS, CdSe, CdTe, MgS, MgSe, GaAs, GaN, GaP, GaSe, GaSb, HgO, HgS, HgSe, An alloy or mixture of HgTe, InAs, InN, InSb, AlAs, AlN, AlP, AlSb, PbO, PbS, PbSe, PbTe, Ge, Si, and any combination thereof.
  • the quantum dots having a core-shell structure may include a single layer or a multilayer structure.
  • the shell includes one or more semiconductor materials that are the same or different from the core.
  • the shell has a thickness of from about 1 to 20 layers.
  • the shell has a thickness of about 5 to 10 layers.
  • two or more shells are included on the surface of the quantum dot core.
  • the semiconductor material used for the shell has a larger band gap than the core.
  • the shell core has a type I semiconductor heterojunction structure.
  • the semiconductor material used for the shell has a smaller band gap than the core.
  • the semiconductor material used for the shell has an atomic crystal structure that is the same as or close to the core. Such a choice is beneficial to reduce the stress between the core shells and make the quantum dots more stable.
  • Examples of suitable luminescent quantum dots using a core-shell structure are:
  • Red light CdSe/CdS, CdSe/CdS/ZnS, CdSe/CdZnS, etc.
  • Green light CdZnSe/CdZnS, CdSe/ZnS, etc.
  • Blue light CdS/CdZnS, CdZnS/ZnS, etc.
  • a preferred method of preparing quantum dots is a colloidal growth method.
  • the method of preparing monodisperse quantum dots is selected from the group consisting of hot-inject and/or heating-up.
  • the preparation method is contained in the document Nano Res, 2009, 2, 425-447; Chem. Mater., 2015, 27(7), pp 2246-2285. The entire contents of the above-listed documents are hereby incorporated by reference.
  • the surface of the quantum dot comprises an organic ligand.
  • Organic ligands can control the growth process of quantum dots, regulate the appearance of quantum dots and reduce surface defects of quantum dots to improve the luminous efficiency and stability of quantum dots.
  • the organic ligand may be selected from the group consisting of pyridine, pyrimidine, furan, amine, alkylphosphine, alkylphosphine oxide, alkylphosphonic acid or alkylphosphinic acid, alkyl mercaptan and the like.
  • organic ligands include, but are not limited to, tri-n-octylphosphine, tri-n-octylphosphine oxide, trihydroxypropylphosphine, tributylphosphine, tris(dodecyl)phosphine, dibutyl phosphite , tributyl phosphite, octadecyl phosphite, trilauryl phosphite, tris(dodecyl) phosphite, triisodecyl phosphite, bis(2-ethylhexyl) phosphate, Tris(tridecyl)phosphate, hexadecylamine, oleylamine, octadecylamine, bisoctadecylamine, octadecylamine, bis(2-ethylhexyl)amine, oleyl
  • the surface of the quantum dot comprises an inorganic ligand.
  • Quantum dots protected by inorganic ligands can be obtained by ligand exchange of organic ligands on the surface of quantum dots. Examples of specific inorganic ligands include, but are not limited to, S 2- , HS - , Se 2- , HSe - , Te 2- , HTe - , TeS 3 2- , OH - , NH 2 - , PO 4 3- , MoO 4 2- , and so on. Examples of such inorganic ligand quantum dots can be found in documents: J. Am. Chem. Soc. 2011, 133, 10612-10620; ACS Nano, 2014, 9, 9388-9402. The entire contents of the above-listed documents are hereby incorporated by reference.
  • the quantum dot surface has one or more of the same or different ligands.
  • the luminescence spectrum exhibited by the monodisperse quantum dots has a symmetrical peak shape and a narrow half width.
  • the better the monodispersity of quantum dots the more symmetric the luminescence peaks are and the narrower the half-width.
  • the quantum dot has a half-width of light emission of less than 70 nanometers; more preferably, the quantum half-width of the quantum dot is less than 40 nanometers; most preferably, the quantum half-width of the quantum dot is smaller than 30 nanometers.
  • the quantum dots have a luminescence quantum efficiency of greater than 10%, preferably greater than 50%, more preferably greater than 60%, and most preferably greater than 70%.
  • the luminescent semiconductor nanocrystals are nanorods.
  • the properties of nanorods are different from those of spherical nanocrystals.
  • the luminescence of the nanorods is polarized along the long rod axis, while the luminescence of the spherical grains is unpolarized (see Woggon et al, Nano Lett., 2003, 3, p509).
  • Nanorods have excellent optical gain characteristics, making them possible to use as laser gain materials (see Banin et al. Adv. Mater. 2002, 14, p317).
  • the luminescence of the nanorods can be reversibly turned on and off under the control of an external electric field (see Banin et al, Nano Lett.
  • nanorods may be preferably incorporated into the device of the present invention under certain circumstances.
  • Examples of the preparation of the semiconductor nanorods are, for example, WO03097904A1, US2008188063A1, US2009053522A1, and KR20050121443A, the entire contents of each of which are hereby incorporated by reference.
  • the inorganic nanomaterial is a perovskite nanoparticle material, particularly a luminescent perovskite nanoparticle material.
  • the perovskite nanoparticle material has the structural formula of AMX 3 wherein A may be selected from an organic amine or an alkali metal cation, M may be selected from a metal cation, and X may be selected from an oxygen or a halogen anion.
  • CsPbCl 3 CsPb(Cl/Br) 3 , CsPbBr 3 , CsPb(I/Br) 3 , CsPbI 3 , CH 3 NH 3 PbCl 3 , CH 3 NH 3 Pb (Cl/Br 3 , CH 3 NH 3 PbBr 3 , CH 3 NH 3 Pb(I/Br) 3 , CH 3 NH 3 PbI 3 and the like.
  • Literature on perovskite nanoparticle materials is NanoLett., 2015, 15, 3692-3696; ACS Nano, 2015, 9, 4533-4542; Angewandte Chemie, 2015, 127(19): 5785-5788; Nano Lett., 2015, 15(4), pp 2640-2644; Adv. Optical Mater. 2014, 2, 670-678; The Journal of Physical Chemistry Letters, 2015, 6(3): 446-450; J. Mater. , 2015, 3, 9187-9193; Inorg. Chem. 2015, 54, 740-745; RSC Adv., 2014, 4, 55908-55911; J. Am. Chem.
  • the inorganic nanomaterial is a metal nanoparticle material.
  • Particularly preferred are luminescent metal nanoparticle materials.
  • the metal nanoparticles include, but are not limited to, chromium (Cr), molybdenum (Mo), tungsten (W), ruthenium (Ru), rhenium (Rh), nickel (Ni), silver (Ag), copper (Cu Nanoparticles of zinc (Zn), palladium (Pd), gold (Au), hungry (Os), ruthenium (Re), iridium (Ir), and platinum (Pt).
  • the types, morphologies and synthetic methods of common metal nanoparticles can be found in: Angew. Chem. Int. Ed. 2009, 48, 60-103; Angew. Chem. Int. Ed. 2012, 51, 7656-7673; Adv. Mater. 2003, 15, No. 5, 353-389; Adv. Mater. 2010, 22, 1781-1804; Small. 2008, 3, 310-325; Angew. Chem. Int. Ed. 2008, 47, 2-
  • the disclosures of the above-cited documents are hereby incorporated by
  • the inorganic nanomaterial has charge transport properties.
  • the inorganic nanomaterial has electron transport capabilities.
  • such inorganic nanomaterials are selected from the group consisting of n-type semiconductor materials.
  • n-type inorganic semiconductor materials include, but are not limited to, metal chalcogen compounds, metal phosphorus group compounds, or elemental semiconductors such as metal oxides, metal sulfides, metal selenides, metal tellurides, metal nitrides, Metal phosphide, or metal arsenide.
  • Preferred n-type inorganic semiconductor materials are selected from the group consisting of ZnO, ZnS, ZnSe, TiO 2 , ZnTe, GaN, GaP, AlN, CdSe, CdS, CdTe, CdZnSe, and any combination thereof.
  • the inorganic nanomaterial has a hole transporting ability.
  • such inorganic nanomaterials are selected from p-type semiconductor materials.
  • the inorganic p-type semiconductor material may be selected from the group consisting of NiOx, WOx, MoOx, RuOx, VOx, CuOx, and any combination thereof.
  • the printing ink according to the present invention comprises at least two and two or more inorganic nanomaterials.
  • the printed electronic composition according to the invention comprises at least one organic functional material.
  • the organic functional materials include, but are not limited to, holes (also called holes) injection or transport materials (HIM/HTM), hole blocking materials (HBM), electron injection or transport materials (EIM/ETM), Electron barrier material (EBM), organic host material (Host), singlet illuminant (fluorescent illuminant), thermally activated delayed fluorescent luminescent material (TADF), triplet illuminant (phosphorescent illuminant), especially luminescent organic metal Complex, organic dye.
  • holes also called holes injection or transport materials
  • HBM hole blocking materials
  • EIM/ETM electron injection or transport materials
  • EBM Electron barrier material
  • organic host material Host
  • singlet illuminant fluorescent illuminant
  • TADF thermally activated delayed fluorescent luminescent material
  • phosphorescent illuminant especially luminescent organic metal Complex, organic dye.
  • Various organic functional materials are described in detail in, for example, WO2010135519A1, US20090134784A1, and
  • the solubility of the organic functional material in the olefin solvent according to the present invention is at least 0.2% by weight, preferably at least 0.3% by weight, more preferably at least 0.6% by weight, still more preferably at least 1.0% by weight, Best at least 1.5wt%.
  • the organic functional material may be a small molecule and a high polymer material.
  • the small molecule organic material means a material having a molecular weight of at most 4000 g/mol, and the material having a molecular weight higher than 4000 g/mol is collectively referred to as a high polymer.
  • the printed electronic composition according to the present invention comprises a functional material that is an organic small molecule material.
  • a printed electronic composition according to the invention wherein said organic functional material comprises at least one host material and at least one illuminant.
  • the organic functional material comprises a host material and a singlet emitter.
  • the organic functional material comprises a host material and a triplet emitter.
  • the organic functional material comprises a host material and a thermally activated delayed fluorescent luminescent material.
  • the organic functional material comprises a hole transporting material (HTM), and more preferably, the HTM comprises a crosslinkable group.
  • HTM hole transporting material
  • organic small molecule functional materials suitable for the preferred embodiment will be described in some detail below (but are not limited thereto).
  • Suitable organic HIM/HTM materials may optionally comprise compounds of the following structural units: phthalocyanine, porphyrin, amine, aromatic amine, biphenyl triarylamine, thiophene, thiophene such as dithienothiophene and thiophene, pyrrole, aniline, Carbazole, azide and azepine and their derivatives.
  • suitable HIMs also include fluorocarbon-containing polymers, conductively doped polymers, conductive polymers such as PEDOT:PSS.
  • An electron blocking layer is used to block electrons from adjacent functional layers, particularly the luminescent layer.
  • the electron blocking material (EBM) of the electron blocking layer (EBL) requires a higher LUMO than an adjacent functional layer such as a light emitting layer.
  • the HBM has a larger excited state level than the adjacent luminescent layer, such as a singlet or triplet, depending on the illuminant, while the EBM has a hole transport function.
  • HIM/HTM materials that typically have high LUMO levels can be used as EBMs.
  • cyclic aromatic amine-derived compounds useful as HIM, HTM or EBM include, but are not limited to, the following general structures:
  • Each of Ar 1 to Ar 9 may be independently selected from the group consisting of a cyclic aromatic hydrocarbon compound such as benzene, biphenyl, triphenyl, benzo, naphthalene, anthracene, phenalrene, phenanthrene, anthracene, anthracene, fluorene, anthracene, anthracene; Heterocyclic compounds such as dibenzothiophene, dibenzofuran, furan, thiophene, benzofuran, benzothiophene, oxazole, pyrazole, imidazole, triazole, isoxazole, thiazole, oxadiazole, evil Triazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, acesulfazine, oxadiazine, hydrazine
  • Ar 1 to Ar 9 may be independently selected from the group consisting of:
  • n is an integer from 1 to 20; X 1 to X 8 are CH or N; and Ar 1 is as defined above.
  • metal complexes that can be used as HTM or HIM include, but are not limited to, the following general structures:
  • M is a metal having an atomic weight greater than 40
  • (Y 1 -Y 2 ) is a two-dentate ligand, Y 1 and Y 2 are independently selected from C, N, O, P and S; L is an ancillary ligand;
  • n is an integer whose value ranges from 1 to the maximum coordination number of the metal; m+n is the maximum coordination number of the metal.
  • (Y 1 -Y 2 ) is a 2-phenylpyridine derivative.
  • (Y 1 -Y 2 ) is a carbene ligand.
  • M is selected from the group consisting of Ir, Pt, Os, and Zn.
  • the HOMO of the metal complex is greater than -5.5 eV (relative to the vacuum level).
  • the example of the triplet host material is not particularly limited, and any metal complex or organic compound may be used as the host as long as its triplet energy is higher than that of the illuminant, particularly the triplet illuminant or the phosphorescent illuminant.
  • metal complexes that can be used as the triplet host include, but are not limited to, the following general structure:
  • M is a metal
  • (Y 3 -Y 4 ) is a bidentate ligand, Y 3 and Y 4 are independently selected from C, N, O, P, and S
  • L is an ancillary ligand
  • m is an integer , the value from 1 to the maximum coordination number of this metal
  • m + n is the maximum coordination number of this metal.
  • the metal complex useful as the triplet host has the following form:
  • (O-N) is a two-tooth ligand in which the metal coordinates with the O and N atoms.
  • M can be selected from the group consisting of Ir and Pt.
  • Examples of the organic compound which can be used as the host of the triplet state are selected from compounds containing a cyclic aromatic hydrocarbon group such as benzene, biphenyl, triphenyl, benzo, anthracene; compounds containing an aromatic heterocyclic group such as dibenzothiophene and diphenyl.
  • a cyclic aromatic hydrocarbon group such as benzene, biphenyl, triphenyl, benzo, anthracene
  • compounds containing an aromatic heterocyclic group such as dibenzothiophene and diphenyl.
  • the triplet host material can be selected from compounds comprising at least one of the following groups:
  • R 1 -R 7 may be independently of one another selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkene, alkyne, aralkyl, heteroalkyl, aryl and heteroaryl, when they are aryl Or a heteroaryl group, which has the same meaning as Ar 1 and Ar 2 described above; n is an integer from 0 to 20; X 1 -X 8 is selected from CH or N; and X 9 is selected from CR 1 R 2 or NR 1 .
  • the example of the singlet host material is not particularly limited, and any organic compound may be used as the host as long as its singlet energy is higher than that of the illuminant, particularly the singlet illuminant or the luminescent illuminant.
  • Examples of the organic compound used as the singlet host material may be selected from the group consisting of a cyclic aromatic compound such as benzene, biphenyl, triphenyl, benzo, naphthalene, anthracene, anthracene, phenanthrene, anthracene, anthracene, fluorene, fluorene, fluorene, An aromatic heterocyclic compound such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, oxazole, carbazole, pyridine Anthraquinone, pyrrole dipyridine, pyrazole, imidazole, triazole, isoxazole, thiazole, oxadiazole, triazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrim
  • the singlet host material can be selected from compounds comprising at least one of the following groups:
  • R 1 may be independently of one another selected from the group consisting of hydrogen, alkyl, alkoxy, amino, alkene, alkyne, aralkyl, heteroalkyl, aryl and heteroaryl;
  • Ar 1 is aryl or a heteroaryl group having the same meaning as Ar 1 defined in the above HTM;
  • n is an integer from 0 to 20;
  • X 1 -X 8 is selected from CH or N; and
  • X 9 and X 10 are selected from CR 1 R 2 or NR 1 .
  • Singlet emitters tend to have longer conjugated pi-electron systems.
  • styrylamine and its derivatives disclosed in JP 2913116 B and WO 2001021729 A1
  • indenoindenes and derivatives thereof disclosed in WO 2008/006449 and WO 2007/140847.
  • the singlet emitter can be selected from the group consisting of monostyrylamine, dibasic styrylamine, ternary styrylamine, quaternary styrylamine, styrene phosphine, styrene ether and arylamine.
  • a monostyrylamine refers to a compound comprising an unsubstituted or substituted styryl group and at least one amine, preferably an aromatic amine.
  • a binary styrylamine refers to a compound comprising two unsubstituted or substituted phenylene The alkenyl group and at least one amine, preferably an aromatic amine.
  • a ternary styrylamine refers to a compound comprising three unsubstituted or substituted styryl groups and at least one amine, preferably an aromatic amine.
  • a quaternary styrylamine refers to a compound comprising four unsubstituted or substituted styryl groups and at least one amine, preferably an aromatic amine.
  • a preferred styrene is stilbene, which may be further substituted.
  • the corresponding phosphines and ethers are defined similarly to amines.
  • An arylamine or an aromatic amine refers to a compound comprising three unsubstituted or substituted aromatic ring or heterocyclic systems directly bonded to a nitrogen. At least one of these aromatic or heterocyclic ring systems is preferably selected from the group consisting of fused ring systems, and preferably at least 14 aromatic ring atoms.
  • Preferred examples thereof are aromatic decylamine, aromatic quinone diamine, aromatic decylamine, aromatic quinone diamine, aromatic thiamine and aromatic quinone diamine.
  • An aromatic amide refers to a compound in which a diaryl arylamine group is attached directly to the oxime, preferably at the position of 9.
  • An aromatic quinone diamine refers to a compound in which two diaryl arylamine groups are attached directly to the oxime, preferably at the 9,10 position.
  • the definitions of aromatic decylamine, aromatic quinone diamine, aromatic thiamine and aromatic quinone diamine are similar, wherein the diaryl aryl group is preferably bonded to the 1 or 1,6 position of hydrazine.
  • Examples of singlet emitters based on vinylamines and arylamines are also preferred examples and can be found in the following patent documents: WO 2006/000388, WO 2006/058737, WO 2006/000389, WO 2007/065549, WO 2007 /115610, US 7250532 B2, DE 102005058557 A1, CN 1583691 A, JP 08053397 A, US 6251531 B1, US 2006/210830 A, EP 1957606 A1 and US 2008/0113101 A1, the entire contents of which are hereby incorporated by reference. This article is incorporated herein by reference.
  • Further preferred singlet emitters may be selected from the group consisting of an indeno-amine and an indeno-diamine, as disclosed in WO 2006/122630, benzoindolo-amine and benzoindolo-diamine , as disclosed in WO 2008/006449, dibenzoindolo-amine and dibenzoindeno-diamine, as disclosed in WO 2007/140847.
  • polycyclic aromatic hydrocarbon compounds in particular derivatives of the following compounds: for example, 9,10-bis(2-naphthoquinone), naphthalene, tetraphenyl, xanthene, phenanthrene , ⁇ (such as 2,5,8,11-tetra-t-butyl fluorene), anthracene, phenylene such as (4,4'-bis(9-ethyl-3-carbazolevinyl)-1 , 1 '-biphenyl), indenyl hydrazine, decacycloolefin, hexacene benzene, anthracene, spirobifluorene, aryl hydrazine (such as US20060222886), arylene vinyl (such as US5121029, US5130603), cyclopentane Alkene such as tetraphenylcyclopentadiene, rub
  • TDF Thermally activated delayed fluorescent luminescent material
  • the thermally activated delayed fluorescent luminescent material is a third generation organic luminescent material developed after organic fluorescent materials and organic phosphorescent materials.
  • Such materials generally have a small singlet-triplet energy level difference ( ⁇ E st ), and triplet excitons can be converted into singlet exciton luminescence by inter-system crossing. This can make full use of the singlet excitons and triplet excitons formed under electrical excitation.
  • the quantum efficiency in the device can reach 100%.
  • the TADF material needs to have a small singlet-triplet energy level difference, typically ⁇ E st ⁇ 0.3eV, preferably ⁇ E st ⁇ 0.2eV, more preferably ⁇ E st ⁇ 0.1eV, and most preferably ⁇ E st ⁇ 0.05eV.
  • TADF has better fluorescence quantum efficiency.
  • TADF luminescent materials can be found in the following patent documents: CN103483332(A), TW201309696(A), TW201309778(A), TW201343874(A), TW201350558(A), US20120217869(A1), WO2013133359(A1), WO2013154064( A1), Adachi, et.al. Adv. Mater., 21, 2009, 4802, Adachi, et. al. Appl. Phys. Lett., 98, 2011, 083302, Adachi, et. al. Appl. Phys. Lett ., 101, 2012, 093306, Adachi, et. al. Chem.
  • TADF luminescent materials are listed in the table below:
  • Triplet emitters are also known as phosphorescent emitters.
  • the triplet emitter is a metal complex of the formula M(L) n , wherein M is a metal atom, and each occurrence of L may be the same or different and is an organic ligand. It is bonded to the metal atom M by one or more positional bonding or coordination, and n is an integer greater than 1, preferably 1, 2, 3, 4, 5 or 6.
  • these metal complexes are coupled to a polymer by one or more positions, preferably by an organic ligand.
  • the metal atom M is selected from the group consisting of transition metal elements or lanthanides or actinides, preferably Ir, Pt, Pd, Au, Rh, Ru, Os, Sm, Eu, Gd, Tb, Dy Re, Cu or Ag is particularly preferably selected from Os, Ir, Ru, Rh, Re, Pd or Pt.
  • the triplet emitter comprises a chelating ligand, ie a ligand, coordinated to the metal by at least two bonding sites, it is particularly preferred to consider that the triplet emitter comprises two or three identical or different bidentates or Multidentate ligand. Chelating ligands are beneficial for increasing the stability of metal complexes.
  • Examples of the organic ligand may be selected from a phenylpyridine derivative, a 7,8-benzoquinoline derivative, a 2(2-thienyl)pyridine derivative, a 2(1-naphthyl)pyridine derivative, or a 2 benzene.
  • a quinolinol derivative All of these organic ligands may be taken Generation, for example by fluorine or trifluoromethyl.
  • the ancillary ligand may preferably be selected from the group consisting of acetone acetate or picric acid.
  • the metal complex that can be used as the triplet emitter has the following form:
  • M is a metal selected from the group consisting of transition metal elements or lanthanides or actinides;
  • Ar 1 may be the same or different at each occurrence, and is a cyclic group containing at least one donor atom, that is, an atom having a lone pair of electrons, such as nitrogen or phosphorus, through which a cyclic group is coordinated to a metal.
  • Ar 2 may be the same or different at each occurrence, and is a cyclic group containing at least one C atom through which a cyclic group is bonded to a metal; Ar 1 and Ar 2 are linked by a covalent bond, Each may carry one or more substituent groups, which may also be linked together by a substituent group; each occurrence of L may be the same or different, is an ancillary ligand, preferably a bidentate chelate ligand, most Desirable is a monoanionic bidentate chelate ligand; m is 1, 2 or 3, preferably 2 or 3, particularly preferably 3; n is 0, 1, or 2, preferably 0 or 1, particularly preferably Ground is 0;
  • triplet emitters Some examples of suitable triplet emitters are listed in the table below:
  • the printed electronic composition according to the present invention comprises a functional material that is a polymeric material.
  • organic small molecule functional materials described above including HIM, HTM, ETM, EIM, Host, fluorescent illuminants, phosphorescent emitters, and TADF can all be included as a repeating unit in a high polymer.
  • the high polymer suitable for the present invention is a conjugated high polymer.
  • conjugated polymers have the following general formula:
  • A can independently select the same or different structural units when appearing multiple times
  • B a ⁇ -conjugated structural unit having a large energy gap, also called a Backbone Unit, selected from a monocyclic or polycyclic aryl or heteroaryl group, preferably selected as a benzene, a bis. Biphenylene, naphthalene, anthracene, phenanthrene, dihydrophenanthrene, 9,10-dihydrophenanthrene, anthracene, diterpene, spirobifluorene, p-phenylacetylene, ruthenium, fluorene, dibenzo-indole And ⁇ , ⁇ and naphthalene and their derivatives.
  • a Backbone Unit selected from a monocyclic or polycyclic aryl or heteroaryl group, preferably selected as a benzene, a bis. Biphenylene, naphthalene, anthracene, phenanthrene, dihydrophenanthrene, 9,10-dihydrophen
  • A: a ⁇ -conjugated structural unit having a smaller energy gap, also called a functional unit, may be selected from hole injection or transport materials (HIM/HTM) including the above, according to different functional requirements.
  • HIM/HTM hole injection or transport materials
  • EIM/ETM Electronic injection or transport material
  • host material Host
  • singlet illuminant fluorescent illuminant
  • structural unit of heavy illuminant phosphorescent illuminant
  • the printed electronic composition according to the present invention comprises a functional material that is a high polymer HTM.
  • the high polymer HTM material is a homopolymer, and preferred homopolymers are selected from the group consisting of polythiophenes, polypyrroles, polyanilines, polybiphenyl triarylamines, polyvinyl carbazoles and derivatives thereof. Object.
  • the high polymer HTM material is a conjugated copolymer represented by Chemical Formula 1, wherein
  • A a functional group having a hole transporting ability, which may be the same or differently selected from the structural unit comprising the hole injection or transport material (HIM/HTM) described above; in a preferred embodiment, A is selected From amines, biphenyls, triarylamines, thiophenes, and thiophenes such as dithienothiophenes and thiophenes, pyrrole, aniline, carbazole, indenocarbazole, arsenazo, pentacene, phthalocyanine, porphyrin and their derivatives Object.
  • HIM/HTM hole injection or transport material
  • R each independently of each other is hydrogen, a linear alkyl group having 1 to 20 C atoms, an alkoxy group or a thioalkoxy group, or a branched or cyclic alkyl group having 3 to 20 C atoms.
  • r 0, 1, 2, 3 or 4;
  • s 0, 1, 2, 3, 4 or 5;
  • Another preferred class of organic functional materials are polymers having electron transport capabilities, including conjugated high polymers and non-conjugated high polymers.
  • the selected polymeric ETM material is a homopolymer, and preferred homopolymers are selected from the group consisting of polyphenanthrene, polyphenanthroline, polyfluorene, polyspiroquinone, polyfluorene, and derivatives thereof.
  • the selected high polymer ETM material is a conjugated copolymer represented by Chemical Formula 1, wherein A can independently select the same or different forms when it is present multiple times:
  • A a functional group having an electron transporting ability, preferably selected from the group consisting of tris(8-hydroxyquinoline)aluminum (AlQ3), benzene, diphenylene, naphthalene, anthracene, phenanthrene, Dihydrophenanthrene, anthracene, diterpene, snail , p-phenylacetylene, anthracene, anthracene, 9,10-Dihydrophenanthrene, phenazine, phenanthroline, ruthenium, fluorene, dibenzo-indenoindole, indenylnaphthalene, benzindene and their derivatives Object
  • AlQ3 tris(8-hydroxyquinoline)aluminum
  • the printed electronic composition according to the present invention comprises a functional material that is a luminescent polymer.
  • the luminescent polymer is a conjugated high polymer having the following general formula:
  • a functional group having a hole or electron transporting ability which may be selected from structural units comprising the hole injection or transport material (HIM/HTM) described above, or an electron injecting or transporting material (EIM/ETM).
  • HIM/HTM hole injection or transport material
  • EIM/ETM electron injecting or transporting material
  • A2 a group having a light-emitting function, which may be selected from structural units including the singlet emitter (fluorescent emitter) and the heavy emitter (phosphorescent emitter) described above.
  • luminescent polymers are disclosed in the following patent applications: WO2007043495, WO2006118345, WO2006114364, WO2006062226, WO2006052457, WO2005104264, WO2005056633, WO2005033174, WO2004113412, WO2004041901, WO2003099901, WO2003051092, WO2003020790, WO2003020790, US2020040076853, US2020040002576, US2007208567, US2005962631, EP 201345477, EP 2001 344 788, DE 10 2004 020 298, the entire disclosure of which is incorporated herein by reference.
  • the high polymer suitable for the present invention is a non-conjugated high polymer.
  • This can be that all functional groups are on the side chain and the backbone is a non-conjugated high polymer.
  • Some of such non-conjugated high polymers useful as phosphorescent or phosphorescent materials are disclosed in U.S. Patent Nos. 7,250,226, B2, JP 2007 059 939 A, JP 2007 211 243 A2, and JP 2007 1975 074 A2, each of which is incorporated herein by reference.
  • Patent applications such as JP2005108556, JP2005285661, and JP2003338375 are disclosed.
  • the non-conjugated high polymer may be a high polymer, and the functional units conjugated to the main chain are linked by non-conjugated linking units.
  • high polymers are in DE102009023154.4 and DE102009023156.0. There is publicity in it. The entire contents of the above patent documents are hereby incorporated by reference.
  • the present invention also relates to a method of preparing a film comprising a functional material by a printing or coating method, wherein any of the printed electronic compositions as described above is applied to a substrate by printing or coating, wherein
  • the printing or coating method may be selected from, but not limited to, ink jet printing, Nozzle Printing, typography, screen printing, dip coating, spin coating, blade coating, roll printing, torsion roll printing. , lithography, flexo printing, rotary printing, spraying, brushing or pad printing, slit-type extrusion coating, etc.
  • the film comprising the functional material is prepared by a method of ink jet printing.
  • Inkjet printers that can be used to print inks in accordance with the present invention are commercially available printers and include drop-on-demand printheads. These printers are available from Fujifilm Dimatix (Lebanon, NH), Trident International (Brookfield, Conn.), Epson (Torrance, Calif), Hitachi Data systems Corporation (Santa Clara, Calif), Xaar PLC (Cambridge, United Kingdom), and Idanit. Technologies, Limited (Rishon Le Zion, Isreal) purchased.
  • the present invention can be printed using Dimatix Materials Printer DMP-3000 (Fujifilm).
  • the invention further relates to an electronic device comprising one or more functional films, wherein at least one of the functional films is prepared by printing an electronic composition according to the invention, in particular by printing or coating.
  • Suitable electronic devices include, but are not limited to, quantum dot light emitting diodes (QLEDs), quantum dot photovoltaic cells (QPVs), quantum dot luminescent cells (QLEEC), quantum dot field effect transistors (QFETs), quantum dot luminescence field effect transistors, quantum dots.
  • QLEDs quantum dot light emitting diodes
  • QPVs quantum dot photovoltaic cells
  • QLEEC quantum dot luminescent cells
  • QFETs quantum dot field effect transistors
  • Quant dot luminescence field effect transistors quantum dots.
  • the electronic device described above is an electroluminescent device or a photovoltaic cell, as shown in FIG. 1, comprising a substrate (101), an anode (102), at least one luminescent layer or light absorbing. Layer (104), a cathode (106).
  • the following is only for the description of the electroluminescent device.
  • the substrate (101) may be opaque or transparent.
  • a transparent substrate can be used to make a transparent light-emitting component. See, for example, Bulovic et al. Nature 1996, 380, p29, and Gu et al, Appl. Phys. Lett. 1996, 68, p2606.
  • the substrate can be rigid or elastic.
  • the substrate can be plastic, metal, semiconductor wafer or glass.
  • the substrate has a smooth surface. Substrates without surface defects are a particularly desirable choice.
  • the substrate may be selected from polymeric films or plastics having a glass transition temperature Tg of 150 ° C or higher, preferably more than 200 ° C, more preferably more than 250 ° C, and most preferably more than 300 ° C. Examples of suitable substrates are poly(ethylene terephthalate) (PET) and polyethylene glycol (2,6-naphthalene) (PEN).
  • the anode (102) may comprise a conductive metal or metal oxide, or a conductive polymer.
  • the anode can easily inject holes into the HIL or HTL or the luminescent layer.
  • the absolute value of the difference between the work function of the anode and the HOMO level or the valence band level of the p-type semiconductor material as the HIL or HTL is less than 0.5 eV, preferably less than 0.3 eV, and preferably less than 0.2eV.
  • the anode material include, but are not limited to, Al, Cu, Au, Ag, Mg, Fe, Co, Ni, Mn, Pd, Pt, ITO, aluminum-doped zinc oxide (AZO), and the like.
  • anode material can be deposited using any suitable technique, such as a suitable physical vapor deposition process, including radio frequency magnetron sputtering, vacuum thermal evaporation, electron beam (e-beam), and the like.
  • a suitable physical vapor deposition process including radio frequency magnetron sputtering, vacuum thermal evaporation, electron beam (e-beam), and the like.
  • the anode is patterned.
  • Patterned ITO conductive substrates are commercially available and can be used to prepare devices in accordance with the present invention.
  • the cathode (106) can comprise a conductive metal or metal oxide.
  • the cathode can easily inject electrons into the EIL or ETL or directly into the luminescent layer.
  • the absolute value of the difference between the work function of the cathode and the LUMO level or the conduction band level of the n-type semiconductor material as EIL or ETL or HBL is less than 0.5 eV, preferably less than 0.3 eV, preferably It is less than 0.2eV.
  • all materials which can be used as cathodes for OLEDs are possible as cathode materials for the devices of the invention.
  • cathode material examples include, but are not limited to, Al, Au, Ag, Ca, Ba, Mg, LiF/Al, MgAg alloy, BaF2/Al, Cu, Fe, Co, Ni, Mn, Pd, Pt, ITO, and the like.
  • the cathode material can be deposited using any suitable technique, such as a suitable physical vapor deposition process, including radio frequency magnetron sputtering, vacuum thermal evaporation, electron beam (e-beam), and the like.
  • the luminescent layer (104) includes at least one luminescent functional material, and the thickness thereof may be between 2 nm and 200 nm.
  • the luminescent layer is prepared by printing the printing ink of the invention, wherein the printing ink comprises at least one luminescent functional material as described above, in particular quantum Point or organic functional material.
  • the light emitting device further comprises a hole injection layer (HIL) or hole transport layer (HTL) (103) comprising an organic HTM or inorganic p-type material as described above.
  • HIL hole injection layer
  • HTL hole transport layer
  • the HIL or HTL can be prepared by printing a printing ink of the present invention, wherein the printing ink comprises a functional material having a hole transporting ability, particularly a quantum dot or an organic HTM material.
  • the light emitting device according to the invention further comprises an electron injection layer (EIL) or electron transport layer (ETL) (105) comprising an organic ETM or inorganic n-type material as described above.
  • EIL electron injection layer
  • ETL electron transport layer
  • the EIL or ETL can be prepared by printing a printing ink of the present invention, wherein the printing ink comprises functional materials having electron transport capabilities, particularly quantum dots or organic ETM materials.
  • the invention further relates to the use of a light emitting device according to the invention in various applications, including, but not limited to, various display devices, backlights, illumination sources, and the like.
  • the two sides of the bottle were stoppered with a rubber stopper.
  • the upper part was connected to a condenser tube, and then connected to a double-row tube, heated to 150 ° C, vacuumed for 40 min, and then passed through a nitrogen gas; 12 mL of a syringe was used.
  • ODE was added to a three-necked flask.
  • 1.92 mL of the solution 1 was quickly injected into a three-necked flask with a syringe for 12 min.
  • After 12 min, 4 mL of the solution was added to the three-necked flask with a syringe.
  • n-hexane was added to the three-necked flask, and then the liquid in the three-necked flask was transferred to a plurality of 10 mL centrifuge tubes, centrifuged to remove the lower layer precipitate, and repeated three times; acetone was added to the liquid after the post-treatment 1 to precipitate Centrifuge, remove the supernatant, leave a precipitate; then dissolve the precipitate with n-hexane, add acetone to precipitate, centrifuge, remove the supernatant, leave a precipitate, repeat three times; finally dissolve the precipitate with toluene, transfer to glass Stored in the bottle.
  • solution 1 Weigh 0.0079 g of selenium and 0.1122 g of sulfur in a 25 mL single-necked flask, measure 2 mL of TOP, pass nitrogen, stir, and reserve, hereinafter referred to as solution 1; weigh 0.0128 g of CdO and 0.3670 g of zinc acetate. Take 2.5mL of OA in a 25mL three-necked flask, plug the two sides of the bottle with a rubber stopper, connect a condenser tube at the top, connect to the double-row tube, place the three-necked flask in a 50mL heating jacket, and vacuum the nitrogen.
  • a mixed solvent of 9.5 g of 3-phenoxytoluene and terpinolene (weight ratio of 40:60) was prepared in a vial.
  • the quantum dots were precipitated from the solution with acetone and centrifuged to obtain a quantum dot solid.
  • 0.5 g of quantum dot solids were weighed into a glove box, added to the solvent system in the vial, and stirred and mixed. After stirring at a temperature of 60 ° C until the quantum dots were completely dispersed, it was cooled to room temperature.
  • the obtained quantum dot solution was filtered through a 0.2 m PTFE filter. Seal and store.
  • 0.5 g of ZnO nanoparticle solids were weighed into a glove box, added to the solvent system in the vial, and stirred and mixed. After stirring at a temperature of 60 ° C until the ZnO nanoparticles were completely dispersed, they were cooled to room temperature.
  • the obtained ZnO nanoparticle solution was filtered through a 0.2 m PTFE filter. Seal and store.
  • the organic functional materials involved in the following examples are all commercially available, such as Jilin Elound (Jilin OLED Material Tech Co., Ltd, WWW.jl-oled.com), or synthesized according to methods reported in the literature. .
  • Example 7 Preparation of organic light-emitting layer material printing ink containing 3-phenoxytoluene and terpinolene
  • the luminescent layer organic functional material comprises a phosphorescent host material and a phosphorescent illuminant material.
  • the phosphorescent host material is selected from the group consisting of carbazole derivatives as follows:
  • the phosphorescent emitter material is selected from the group consisting of ruthenium complexes as follows:
  • a mixed solvent of 9.8 g of 3-phenoxytoluene and terpinolene (weight ratio of 40:60) was prepared in a vial. 0.18 g of the phosphorescent host material and 0.02 g of the phosphorescent emitter material were weighed into a glove box, added to the solvent system in the vial, and stirred and mixed. After stirring at a temperature of 60 ° C until the organic functional material was completely dissolved, it was cooled to room temperature. The obtained organic functional material solution was filtered through a 0.2 m PTFE filter. Seal and store.
  • Example 8 Preparation of organic light-emitting layer material printing ink containing 3-phenoxytoluene and terpinolene
  • the luminescent layer organic functional material comprises a fluorescent host material and a fluorescent illuminant material.
  • the fluorescent host material is selected from the group consisting of the following spiro derivatives:
  • the fluorescent emitter material is selected from the group consisting of:
  • a mixed solvent of 9.8 g of 3-phenoxytoluene and terpinolene (weight ratio of 40:60) was prepared in a vial.
  • 0.19 g of fluorescent host material and 0.01 g of phosphor material were weighed into a glove box, added to a solvent system in a vial, and stirred and mixed. After stirring at a temperature of 60 ° C until the organic functional material was completely dissolved, it was cooled to room temperature.
  • the obtained organic functional material solution was filtered through a 0.2 m PTFE filter. Sealed and saved
  • Example 9 Preparation of organic light-emitting layer material printing ink containing 3-phenoxytoluene and terpinolene
  • the luminescent layer organic functional material comprises a host material and a TADF material.
  • the host material is selected from the group consisting of the following structures:
  • the TADF material is selected from the group consisting of the following structures:
  • a mixed solvent of 9.8 g of 3-phenoxytoluene and terpinolene (weight ratio of 40:60) was prepared in a vial. 0.19 g of the host material and 0.01 g of the TADF material were weighed in a glove box, added to the solvent system in the vial, and stirred and mixed. After stirring at a temperature of 60 ° C until the organic functional material was completely dissolved, it was cooled to room temperature. The obtained organic functional material solution was filtered through a 0.2 m PTFE filter. Sealed and saved
  • Example 10 Preparation of hole transport material printing ink containing 1-tetralone and terpinolene
  • the printing ink comprises a hole transport layer material having a hole transporting ability.
  • the hole transporting material is selected from the following triarylamine derivatives:
  • 0.2 g of the hole transporting material was weighed into a glove box, added to the solvent system in the vial, and stirred and mixed. After stirring at a temperature of 60 ° C until the organic functional material was completely dissolved, it was cooled to room temperature.
  • the obtained organic functional material solution was filtered through a 0.2 m PTFE filter. Seal and store.
  • the viscosity of the functional material ink was tested by a DV-I Prime Brookfield rheometer; the surface tension of the functional material ink was tested by a SITA bubble pressure tomometer.
  • the functional material ink obtained in Example 5 had a viscosity of 3.8 ⁇ 0.5 cPs and a surface tension of 32.8 ⁇ 0.5 dyne/cm.
  • the functional material ink obtained in Example 6 had a viscosity of 4.6 ⁇ 0.5 cPs and a surface tension of 34.5 ⁇ 0.3 dyne/cm.
  • the functional material ink obtained in Example 7 had a viscosity of 3.9 ⁇ 0.5 cPs and a surface tension of 32.1 ⁇ 0.5 dyne/cm.
  • the functional material ink obtained in Example 8 had a viscosity of 4.0 ⁇ 0.3 cPs and a surface tension of 33.2 ⁇ 0.5 dyne/cm.
  • the functional material ink obtained in Example 9 had a viscosity of 3.9 ⁇ 0.5 cPs and a surface tension of 32.4 ⁇ 0.5 dyne/cm.
  • the functional material ink obtained in Example 10 had a viscosity of 4.8 ⁇ 0.5 cPs and a surface tension of 33.8 ⁇ 0.2 dyne/cm.
  • the functional layer in the light-emitting diode such as the light-emitting layer and the charge transport layer, can be prepared by inkjet printing using the printing ink containing the functional material based on the olefin organic solvent system prepared above, and the specific steps are as follows.
  • the ink containing the functional material is loaded into an ink tank which is assembled to an ink jet printer such as Dimatix Materials Printer DMP-3000 (Fujifilm).
  • the waveform, pulse time and voltage of the jetted ink are adjusted to optimize ink jetting and to stabilize the ink jet range.
  • the substrate of the OLED/QLED is 0.7 mm thick glass sputtered with an indium tin oxide (ITO) electrode pattern.
  • ITO indium tin oxide
  • the HIL/HTL material is then inkjet printed into the well and the solvent is removed by drying at elevated temperature in a vacuum to obtain a HIL/HTL film. Thereafter, the printing ink containing the luminescent functional material is ink-jet printed onto the HIL/HTL film, and the solvent is removed by drying at a high temperature in a vacuum atmosphere to obtain a luminescent layer film.
  • the printing ink containing the functional material of the electron transporting property is then ink-jet printed onto the luminescent layer film, and the solvent is removed by drying at a high temperature in a vacuum atmosphere to form an electron transport layer (ETL).
  • ETL electron transport layer
  • ETL electron transport layer

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  • Materials Engineering (AREA)
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  • Inks, Pencil-Leads, Or Crayons (AREA)
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Abstract

Composition pour électronique imprimée comprenant au moins un matériau fonctionnel et au moins un solvant à base d'oléfine, en particulier un solvant terpénique. L'invention concerne également un dispositif électronique comprenant ladite composition, et un procédé de préparation d'un film mince de matériau fonctionnel.
PCT/CN2016/099785 2015-11-12 2016-09-23 Composition pour électronique imprimée, dispositif électronique la comprenant, et procédé de préparation d'un film mince de matériau fonctionnel WO2017080318A1 (fr)

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Cited By (4)

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CN107287656A (zh) * 2017-06-13 2017-10-24 华中科技大学 一种iii‑v族量子点诱导生长钙钛矿晶体的方法
CN112310330A (zh) * 2020-10-30 2021-02-02 北京京东方技术开发有限公司 一种量子点材料、量子点发光器件、显示装置及制作方法
US11737343B2 (en) 2018-09-17 2023-08-22 Excyton Limited Method of manufacturing perovskite light emitting device by inkjet printing
CN112310330B (zh) * 2020-10-30 2024-06-04 北京京东方技术开发有限公司 一种量子点材料、量子点发光器件、显示装置及制作方法

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CN113122063A (zh) * 2019-12-30 2021-07-16 Tcl集团股份有限公司 量子点墨水、量子点薄膜的制备方法
CN115851032B (zh) * 2022-12-23 2023-12-22 北京印刷学院 一种电致发光柔版印刷油墨及其制备方法

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CN1379804A (zh) * 1999-08-31 2002-11-13 剑桥显示技术有限公司 沉积发光聚合物层的配方
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CN105038408A (zh) * 2015-08-14 2015-11-11 广州华睿光电材料有限公司 印刷油墨及应用其印刷而成的电子器件

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US20050173680A1 (en) * 2004-02-10 2005-08-11 Haixin Yang Ink jet printable thick film ink compositions and processes
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CN1379804A (zh) * 1999-08-31 2002-11-13 剑桥显示技术有限公司 沉积发光聚合物层的配方
CN102408776A (zh) * 2010-08-24 2012-04-11 精工爱普生株式会社 成膜用油墨、成膜方法、液滴喷出装置、发光元件的制造方法、发光元件、发光装置及电子设备
CN105038408A (zh) * 2015-08-14 2015-11-11 广州华睿光电材料有限公司 印刷油墨及应用其印刷而成的电子器件

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Publication number Priority date Publication date Assignee Title
CN107287656A (zh) * 2017-06-13 2017-10-24 华中科技大学 一种iii‑v族量子点诱导生长钙钛矿晶体的方法
CN107287656B (zh) * 2017-06-13 2018-02-27 华中科技大学 一种iii‑v族量子点诱导生长钙钛矿晶体的方法
US11737343B2 (en) 2018-09-17 2023-08-22 Excyton Limited Method of manufacturing perovskite light emitting device by inkjet printing
CN112310330A (zh) * 2020-10-30 2021-02-02 北京京东方技术开发有限公司 一种量子点材料、量子点发光器件、显示装置及制作方法
CN112310330B (zh) * 2020-10-30 2024-06-04 北京京东方技术开发有限公司 一种量子点材料、量子点发光器件、显示装置及制作方法

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